Tag | Content |
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EnhancerAtlas ID | HS091-04152 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr1:226314380-226317200 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EWSR1-FLI1 | MA0149.1 | chr1:226317086-226317104 | TCTGCCTTCCATCCTTCT | - | 6.01 | Hnf4a | MA0114.3 | chr1:226315652-226315668 | CGGGTCAAAGTCCTCT | + | 6.49 | STAT3 | MA0144.2 | chr1:226315755-226315766 | CTTCCCAGAAG | - | 6.14 |
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| Number of super-enhancer constituents: 25 | ID | Coordinate | Tissue/cell |
SE_10465 | chr1:226314329-226317263 | CD19_Primary | SE_11118 | chr1:226314228-226323738 | CD20 | SE_23364 | chr1:226314431-226316913 | Colon_Crypt_1 | SE_23849 | chr1:226314482-226315331 | Colon_Crypt_2 | SE_23849 | chr1:226315334-226316161 | Colon_Crypt_2 | SE_23849 | chr1:226316204-226316855 | Colon_Crypt_2 | SE_24831 | chr1:226314416-226316628 | Colon_Crypt_3 | SE_26794 | chr1:226314386-226317368 | Esophagus | SE_31597 | chr1:226314394-226317203 | Gastric | SE_41844 | chr1:226314696-226315324 | LNCaP | SE_41844 | chr1:226315457-226316066 | LNCaP | SE_41844 | chr1:226316166-226316615 | LNCaP | SE_43265 | chr1:226314581-226317218 | Lung | SE_43763 | chr1:226314330-226317236 | MM1S | SE_47729 | chr1:226314790-226315311 | Pancreas | SE_47729 | chr1:226315339-226316040 | Pancreas | SE_47729 | chr1:226316205-226316603 | Pancreas | SE_50502 | chr1:226314371-226317219 | Sigmoid_Colon | SE_52861 | chr1:226314391-226316889 | Small_Intestine | SE_56941 | chr1:226314700-226316129 | VACO_400 | SE_56941 | chr1:226316193-226316621 | VACO_400 | SE_62016 | chr1:226296810-226321627 | Toledo | SE_63137 | chr1:226295246-226322063 | Tonsil | SE_65669 | chr1:226312586-226317084 | Pancreatic_islets | SE_67238 | chr1:226314330-226317236 | MM1S |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 7 | Chromosome | Start | End |
chr1 | 226314917 | 226315002 | chr1 | 226315055 | 226316024 | chr1 | 226316027 | 226316129 | chr1 | 226314646 | 226315237 | chr1 | 226315631 | 226315825 | chr1 | 226315308 | 226315548 | chr1 | 226316204 | 226316800 |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I226126 | chr1 | 226314498 | 226317175 |
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Enhancer Sequence | CGGGAGGCTG AGGCAGAAGA ATGGCATGAA CCTGGGAGGT GGAGGTTGCA GTGAGCTGAG 60 ATCGCGCCAC TGCACTCCAG CCTGGGCGAC AGAGCAAGAA TCCGTCTAAA AAAAAAAGAG 120 AGAGTCCCAG TGCTAAAACT GAGAGTCCTG GGCAAACTGG AACAATTGAT CACACAATAA 180 AGTGGGGGTT CTTGGGCTGG GTATGGAGGC TCATGCTTAT AATCTCAGTG CTTTGGGAGG 240 CCAAGGTGGA AGGATTGCTT GAGCCCAGGG CTTCAAGACC AGCCTGGACA ACATAGCAAG 300 ACCCTATCTC TACAAAAGAA AAAACAAGCA CACACTTGTA GTCCCAGCTA CTTGGGAGGC 360 TGAGGCAGGA GGACTGCTTA AGGCCAGGAG GTGGAGGTTG CAATGGGCTA TGATGGCACC 420 TCTGCACTCC AGCCTCAGTG ACAGAGCAAA ACCTCATTTT GAAAACACAC ACATGAGGGG 480 CGCTGGGAAT AGCCGCTCAT GTCGGCTGAC GGAGCGGTGT GGGGCCGCAT GCGAAGCTGC 540 CTCCGCGCCT TCCCCGAGCG GCTGGCCGCC TGCGGGGCCG AGTAAGGACT TCTGCGCGCG 600 GGAGTTCGAG GCCCTGCGGA GCTGCTTCGC CGCCGCGGCC AAGAAGACGC TGGAGGGAGG 660 CTGTTAGGAG GGACTCTGAG CTTCACACCT GTCTGCTGCC GTGGTTGCAG AGCCCTAGTC 720 CTGATGGCCC CCGGTGGCAT ACATTGAATG CCTAGGGCAG AAAGGAAGTG GGAATGGCGA 780 AGATGTGACG TGCCTCGGTG TTAGATACTG TTTCTTCTTA ACAAGTTGAG GCGTGGGTAG 840 AGCAGGAACT GGTTTTCCAG CATTGTGTCC GTAAACCTGA GTCAGAATAA GATGTAACAG 900 AAGCCAGATA AAGACTCTGT CAAATCCTGC AAAAAAAAAA AAAAGAAAAA AAAGAAAACA 960 CACACACACA CACATGCACA CAATGCATAA AGTGTTTCTG AAACTTTGGT GTGCATGAGA 1020 GACACCTGGG GACTTACAAA AACACAGATG GCTGGCCCCA CCCTAGAGTT TCTAATTTAG 1080 TAGGTCCAGG GTGGGGTCCG GTAATTTGCA TTTCTAACAA GTTTCCTGAT ACTGCTGCTG 1140 TTGCTCTTGG TTGGGGCCCA AACTTCCAGA ACAACTGGTC TGAATGAAGG GCTGGGTCCG 1200 GGACCTGCAA GTCCCACTGT GCTGCTTGCC CCGGTACCTC CTCCTAAGTC TGGCCCAGCA 1260 GGAAACGGAG CGCGGGTCAA AGTCCTCTCA CAGTCAACCA GGAGAAACCT GTGTCTTCCT 1320 GGCAGGGTGG CTGGGTGCTA TGGAAACAAG GCTCAGCCCA GAAGTGCCCA GCCTCCTTCC 1380 CAGAAGCAAC TTCAGCCTCT AGGGGAGGAG TGAAGTGAAC AAACAAACGG AAGGGCAGAG 1440 CTCAGTTCCT GGATGGAAGC GGCACCTGCA TGGAAGCGCC CTCAGCAACC TCAGGGCCCA 1500 GACTTCCGGG AAAGTCTCAC AGGGCCCCTG GCTTGAGTTT TGGAGCTGGA AGGGAACTTT 1560 GCAATCTTGG TTCAACTTTT TGTTTTATTT TCTGAGATGA ATCCTCGCTC TGTTGCCCAG 1620 GGTGGGGTGC AGTGGCGCAA TCTCGGCTCA CTGCAACCTC CGCCTCCCGG GTTCCAGCGA 1680 TGCTCCTGCC TCAGCCTCCT GAGTAGCTGG GATCACAGGT GCCTGCCACC ACGGTTGGCT 1740 AAATTTTGTA TTTTTAGTAG AGATGGGGGT TTCACCATGT TGGCCAGGCT GGTCTCGAAC 1800 TCCTTACCTC AGGTGATCCG CCCACCTCTG CCTTCCAAAG TGCTGGGATT ACAGGCATGA 1860 GCCACCGTGC CCGGCCCAGT ACATCTTTTA ACTGGGCTGT GAATGACACG ACTTGCTAAG 1920 ACCTGCCCAC TAAGAATGAG CTGCAGCCAG CACAATGTTG TCCGCTTCCA GCCACTTTCC 1980 TAGATACTCC TCCATTCCTC AGATTCCAGC CCCCACCCCA GCCTGGAACG CCCACAGTGC 2040 TTTTATCACA GCTCTTAACT CCACTTGGTT CCCCAAAGCT ATGAGCCCAC ATACCACCTC 2100 CCAGGGCTAC AACACTTTGG GTTTCTCAGA CACTGTCAAC ACTAAGCAGC ATGAACTGCA 2160 GGACACACAG GACAGCTGGA GAGGGGCAGT GAGTCACTGT GTCATAGTCC TGCCCAAATT 2220 CCAATGTTGA AATTGCAGAA GCCTGGGGCC CACCCTAGAG AATCTGATTC AGCAGGTTGG 2280 AGGGGGGGCC CAGGCACTGA TATTTTCAAG AGCCCTGGGT GATGTGGATG CCGATAGCAC 2340 TGGCTGCATG CTGAGAAACA CTGCCGATAG CATCATCTTC CACAGAAGGC CACCCAGGAA 2400 GAGATGATGA GGTGACAGAA CTTCATCACC CAACTCAAGA AGGCTTGGGA GGAAGGGGTA 2460 ATTTATTGGT TCTAAGCCCA GACCATGGAC AAAACAGAGT GCTATGGTTC AAATGTCCCC 2520 AGCAATGTTC ATGTTGAAAT GTAATTGCCG TTGTGATGGT GGCATTGGCA GGTGGGGCCT 2580 TTGCAAGGTA ATTAGGTTAT GAGGGCTCTG CCCTCAGGAA TGGATCCATG CCATCATCTC 2640 TGGAGTGGGT TCTTGATAAA AAGGATGATT CTGGACCACT TCCCTCTCAT GTCTCACATG 2700 CTTACCTCTG CCTTCCATCC TTCTGCCATG GTGGGGCCCT CACAAGATGC TGGTGCCATG 2760 CTCTTGGACT TTCCAGCCTC CAGGACTGTG GGAAATCAAT TTCTTTTCCA CCCAGTCTGT 2820
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